ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.990T>C (p.Ser330=)

dbSNP: rs2124479772
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001455600 SCV001659364 likely benign Wilms tumor 1 2023-11-19 criteria provided, single submitter clinical testing

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